Amino citric acid derivatives

ABSTRACT

Amino citric acids and esters, and lactams thereof, are useful for the control of lipogenesis.

United States Patent Guthrie et al. Mar. 4, 1975 AMINO CITRIC ACID DERIVATIVES [51] int. Cl C07d 27/08 Inventors: Robert G e, Fleld of Search i Richard Wightman Kierstead, North Caldwell, both of NJ. [561 References Cited 73 Assignee: Hoffman-La Roche Inc., Nutley, UNITED STATES PATENTS Ni 3,133,082 5/1964 Wu et a1. 260/326-45 X Filed: 1974 Primary Examiner-Joseph A. Narcavage [21] APP] No: 435 146 Attorney, Agent, or Firm-Samuel L. Welt; Jon S.

Saxe; George M. Gould Related U.S. Application Data [62] Division of Ser. No. 204,290. Dec. 2, 1971, Pat. No. [57] ABSTRACT Amino citric acids and esters, and lactams thereof, are

52 U.S. Cl. 260/326.45, 260/349 260/534 E useful for the Control of lipogenesis' 8 Claims, N0 Drawings AMINO CITRIC ACID DERIVATIVES mulas depicted herein as drawn do not illustrate the relative or absolute stereochemistry of the particular mol- This is a division, of application Ser. No. 204,290 ecules. It should be understood,however, that allof the filed Dec. 2, 1971, now U.S. Pat. No. 3,799,951. compounds described herein exist in two relative ste- 5 reochemical forms: a threo and erythro form. To facili- BRIEF DESCRIPTION OF THE INVENTION tate the description of stereochemical transformations The present invention relates to novel compounds of reported herein, the threo and erythro nomenclature as the formulas defined by Cram et al., J. Amer. Chem. 500., vol. 74, NH page 5828 (1952) and by Prelog et al., Expw'ientia, vol. 2 l2, page 81 (1956) has been adopted. Each of these CHCO R Ia relative stereochemical forms exists as a racemate and the two optical antipodes, and the formulas shown herein are meant to include all of the isomeric and an- C l CHQCOQR tipodal forms of the compounds depicted. The prepara- OH tion of sulfonyl ester of formula ll and epoxide of for and mula III is described in the U.S. patent application of Guthrie, et al., filed of even date herewith, entitled Citric Acid Derivatives, (Case Docket No. 3293).

H Sulfonyl ester, compound II, can be converted to R0 6 N azide-alcohol of formula IV by treatment with an alkali 0 metal azide such as, for example, sodium azide. The re- H Ib action may be carried out in any inert organic solvent,

such as for example, lower alkanols, e.g. methanol or H0 CO R as ethanol; ketones, e.g. acetone; organic amides, e.g. 2 N,N-dimethyl formamide; and so forth. The reaction temperature can range from about 20 to 150C. A pre- Wherem ferred reaction temperature is in the range of from all R groups are hydrogen or the same lower alkyl, about to about 100C. Surprisingly, it has been and the stereoisomers, optical antipodes and pharmafound that the l t fth lf l group by ceutically acceptable salts thereof, which compounds the dzido group Occurs with retention f configuration ihhlhh fatty acid Synthesis in biological Systems and are Thus, for example, threo-mesylate of formula II affords thus hsefhl in treatment of h y and in Correcting threo-azide of formula IV. it has been found that, dur- Cohdhlohs of lipid hhhormahhesing the course of the reaction, the epoxide of formula AS used throughout the Specification and the P' III is an intermediate,that is,adouble inversion ofconpended Claims the term lower shall mean a figuration amounting to net retention of configuration straight or branched chain hydrocarbon group containccurg Thus for exa nple threoqnegylate goes ing no unsaturation and having up to and including 8 through erythro-epoxide which then opens to afford carbon atoms, such as methyl, ethyl, hexyl, isopropyl, threo-azide. The epoxide of formula III is not normally tert.-butyl and so forth. The term aryl" shall mean isolated during the reaction but its presence can be dephenyl or naphthyl which may be substituted with one 40 tected by spectral and/or chromatographic methods. of the following groups: halogen (i.e. chlorine, bro- Alternatively, one may start with the epoxide of form v o n or fl lower alkyl, hydroxy, lower mula Ill and treat it with an alkali metal azide under the alkoxy or nitro. aforedescribed reaction conditions to obtain the de- The preparation ofcompounds offormulasla and lb sired azide. Following the above reasoning, threois illustrated in Reaction Scheme A. The structural forepoxide affords erythro-azide, and so forth.

REACTION SCHEME A N l t I (iIHCO R E O/(IIHCOZR' faco a' R'O c l ca co a c\ /c\ 2 22 R00 cacon' R'OC l cacoa' on (II) 2 2 2 (III) 2 on 2 2 (Iv) NHQ paco a H c 2 N co 1/ l cn co a o 2 OH 2 2 H (Ia-1) no (ID-1) 7 2 2 I H prico a' R'o c N C H R'O2C/|\CH2CO2R' (Ia-2) on no wherein all R groups are the same lower alkyl and X is lower alkylsulfonyl or aryl sulfonyl.

In the next step, the azido alcohol of formula IV is reduced to amino alcohol of formula la-2. A preferred method of reduction of the azido group to the amino group is catalytic hydrogenation. Suitable catalysts are metal-comprising catalysts, such as palladium, platinum, rhodium, nickel, and the like. The catalyst may be unsupported or may be present on a support such as carbon, asbestos, barium sulfate, strontium carbonate, and so forth. A preferred catalyst is palladium supported on carbon. Any inert organic solvent may be utilized as a reduction medium, for example, alcohols, e.g. methanol or ethanol; ethers, e.g. tetrahydrofuran or dioxane; hydrocarbons, e.g. hexane or benzene; and so forth. Preferred solvents are lower alcohols, e.g. methanol or ethanol. The parameters of temperature and pressure are not narrowly critical. The temperature may range from about room temperature to about 100C, and the pressure from atmospheric pressure to about 50 atmospheres. Generally, a temperature of about room temperature and a pressure of about 3 atmospheres is utilized. The hydrogenation reaction may be conducted in the presence of an added strong acid such as a mineral acid, e.g. hydrogen chloride, which serves to trap the amine as it is formed. In a preferred hydrogenation reaction about 1 equivalent of mineral acid is present in the reaction mixture.

The amino citric acids of formula la-2 may be converted to those of formula la-l by hydrolysis of the ester functions. The hydrolysis may be carried out in aqueous media in the presence of a strong acid or a strong base.

The compounds of formulas Ia-l and 111-2 may be cyclized to the corresponding lactams of formulas lb-l and lb-2, respectively, in a variety of ways. In one example, the free amine of formula la-l or formula la-2 may be heated in an inert solvent to effect the cyclization. Suitable solvents include alcohols, e.g. methanol or ethanol; ethers, e.g. tetrahydrofuran or dioxane; hydrocarbons, e.g. toluene; and so forth. A reaction temperature of from about 50 to 100 is operable, althuogh heating at the reflux point of the solvent is generally preferred. This cyclization technique is not preferred for the cyclization of the threo-amino alcohol because some isomerization of the threo-amino alcohol to the erythro-amino alcohol occurs. A preferred method is to pyrolyze the acid addition salt of the amino alcohol. It is most preferable to utilize the same acid addition salt obtained from the hydrogenation of the azide in the presence of acid. The pyrolysis is conveniently effected in the dry state by heating the acid addition salt above its melting point until cyclization occurs. A high-boiling inert organic solvent can be employed as a diluent, if desired, although this is not normally preferred.

Lactams of formulas lb-l and lb-2 can be interconverted by conventional esterification and saponification techniques.

Optically active compounds of formulas la and lb may be prepared either by utilizing optically active starting materials of, for example, formula II, or by optical resolution.'Compounds of formula la-2 may be resolved utilizing an optically active acid, such as an antipode of, for example, camphorsulfonic acid, tartaric acid, and so forth. The lactam of formula lb-l may be resolved utilizing an optically active base, such as for example, cinchonidine, a-methylbenzylamine, and so forth.

The compounds of formulas la and lb are useful for inhibiting fatty acid synthesis in biological systems. The

biological systems in which the compounds of the present invention may be used include those which contain citrate'cleavage enzyme. Preferred biological systems are mammals, particularly non-ruminating mammals.

The inhibition of fatty acid synthesis in biological systems, by the use of the compounds ofthe present invention is believed to arise from the inhibition of citrate cleavage enzyme contained in such systems. The cleavage of citrate is catalyzed by citrate cleavage enzyme according to the stoichiometry: citrate CoA ATP acetyl CoA oxaloacetate ADP P,.

I In the conversion of carbohydrates and various amino acids to fat by non-ruminating mammals, citrate is the major source of acetyl co-enzyme A which is utilized for the synthesis of fatty acids. Citrate is formed in the mitochondria by the citrate synthase reaction. It is then metabolized via the citric acid cycle. Under con ditions when energy intake exceeds energy demand some citrate is diverted to the extm-mitochondrial space ofthe cell where it is used for fatty acid synthesis, that is to say, for energy storage.

The novel compounds of formulas la and lb of the present invention are thus useful in the treatment of obesity and in the correction of lipid abnormalities. The compounds of formulas la and lb may also be utilized in the form of the pharmaceutically acceptable nontoxic salts. When R is hydrogen, a salt can be formed with a suitable base. Preferred salts for this purpose include the alkali metals, e.g. sodium or potassium; the alkaline earth metals, e.g. calcium; or complex salts such as ammonium or substituted ammonium salts such as a mono-, di or tri-alkyl ammonium salt or a mono-, dior tri-hydroxy-alkyl ammonium salt. Com pounds of formula la can also form salts with suitable acids. Preferred acids include mineral acids, e.g. hydrochloric acid; organic acids, e.g. maleic acid, acetic acid, and so forth.

The compounds can be made up in the form of conventional pharmaceutical preparations; for example, the aforesaid compounds can be mixed with organic or inorganic inert pharmaceutical carriers suitable for parenteral or enteral administration such as, for example, water, gelatin, lactose, starch, magnesium stearate, talc, vegetable oil, gums or the like. They can be administered in conventional pharmaceutical forms, e.g. solid forms, for. example, tablets, capsules, dragees. suppositories, or the like; or in liquid forms, for example, solutions suspensions, or emulsions. Moreover, the pharmaceutical compositions containing the compounds of this invention can be subjected to the conventional pharmaceutical expedients, such as sterilization, and can contain conventional pharmaceutical excipients such as preservatives, stabilizing agents, emulsifying agents, salts for the adjustment of osmotic pressure or buffers. The compositions can also contain other therapeutically active materials.

A suitable pharmaceutical dosage unit can contain from about 15 to 600 mg. of the aforesaid compound.

Suitable parenteral dosage regimens in mammals comprise from about 1 mg/kg to about 25 mg/kg per day. However, for any particular subject, specific dosage regimens should be adjusted according to the individual need and the professional judgment of the person administering or supervising the administration of the aforesaid compounds. It is to be understood that the dosages set forth herein are exemplary only that they do not, to any extent, limit the scope or practice of the invention.

The present invention may be more clearly illustrated by the following examples. All temperatures are stated in degrees Centigrade.

EXAMPLE 1 (i)-Threo-l-azido'2-hydroxy-l,2,3- propanetricarboxylic acid, trimethyl ester a. From the (i)-threo-mesylate A solution of sodium azide (5.2 g.) in water ml.) was added to a stirred solution of (i)-threo-l-mesyloxy-Z-hydroxy- 1 l,2.3-propanetricarboxylic acid, trimethyl ester (13.12 g.) in ethanol (100 ml.) and the mixture was heated at reflux for 45 minutes. The reaction mixture was cooled and most of the solvent was removed under reduced pressure. The residue was partitioned using chloroform (2 X 250 ml.) and water 100 ml.) The combined chloroform extracts were washed with water (100 ml.) then were dried (MgSO and concentrated to dryness to give the azide as an oil. It was identical to that obtained from the (i)-erythro epoxide (see below).

b. From the (i)-erythro epoxide A solution of sodium azide (1.12 g.) in water (5 ml.) was added to a solution of (i)-erythro-l,2-epoxy-1,2,3 propanetricarboxylic acid, trimethyl ester [(i)-erythro-epoxyaconitic acid, trimethyl ester] (1.89 g.) in ethanol (20 ml.) containing acetic acid (540 mg). The mixture was heated at reflux for minutes then cooled and concentrated in vacuo. The resulting residue was taken up in chloroform and the chloroform solution was washed with water (3 x). The aqueous layers were backwashed with chloroform and the combined organic extracts were dried (MgSO and evaporated under reduced pressure to give the azide as an oil. The oil was triturated with cold ether to give the azide as a white solid, mp 4346. The analytically pure material was obtained from the same solvent, mp 4748.

Anal. Calcd. for C H MO C. 39.28; H 4.76; N. 15.27. Found: C. 39 55; H. 4.65; N. 15.32.

EXAMPLE 2 (i)-Threo-l-amino-2-hydroxy-1,2,3- propanetricarboxylic acid, trimethyl ester, hydrochloride Anal. Calcd. for C,,H,;,NO;.HC1: C. 37.84; H. 5.65: N. 4.90;

Found: C. 37.97; H. 5.70; N. 4.92; Cl. 12.43.

EXAMPLE 3 (i)-Threo-1-amino-2-hydroxy1,2,3- propanetricarboxylic acid, y lac'tam. dimethyl ester 3.5 g. Of the (i)-amine hydrochloride prepared as in Example 2 was placed in a 125 ml. Erlenmeyer flask and the vessel was flushed with argon. The flask was then placed in an oil bath preheated to 180. A slow stream of argon was swept through the flask during the 0 reaction. After the compound had. melted and the bubbling had ceased (2-3 minutes) the flask was cooled and the pyrolysate was dissolved in ethyl acetate (with the help of a small volume of methanol) and placed on a column of Florisil (60-100 mesh; g.) and eluted with 2% methanol in ethyl acetate. Concentration of the eluates (1800 ml.) furnished the lactam. Crystallization from methanol-ethyl acetate afforded pure lactam, mp l446. The analytical sample was obtained from the same solvent system. mp 144-6.

Anal. Calcd. for C,.H NO..: C. 44.24; H, 5.11; N. 6.45. Found: C, 44.45; H, 5.28; N. 6.33.

EXAMPLE 4 A solution of potassium t-butoxide (225 mg.; 2.0 mmole) in dry methanol (10 ml.) was added to a solution of the hydrochloride prepared as in Example 3 (571 mg.; 2.0 mmol) in methanol 10 ml.) and the solution was heated at reflux for 2 hours. The solvent was removed in vacuo and the solid residue was extracted with several portions of hot ethyl acetate (3 X 30 ml.). The combined extracts were decolorized (charcoal), then filtered and evaporated to dryness under reduced pressure to give an oil. Analysis of this oil showed it to be a mixture of the three-lactam and the (i)-erythrolactam.

EXAMPLE 5 (i)-Threol -amino-2-hydroxy-l ,2,3- propanetricarboxylic acid, 7 lactam A solution of the threo-diester lactam prepared as in Example 4 (540 mg; 2.5 mmol) in IN sodium hydroxide solution (6.25 ml.; 6.25 mmol) was allowed to stand at room temperature for 25 minutes. The solution was then passed through a column of cation exchange resin (Amberlite IRA 10 ml.). The acidic eluate was concentrated in vacuo to give a white solid. Recrystallization from methanol-carlmn tetrachloride furnished the analytically pure material. mp 222-3.

Anal. Calcd. for C,.H,NO..: C. 38.11; H. 3.73; N. 7.41.

Found: C. 38.01; H. 3.62; N. 7.33.

EXAMPLE 6 (i)-Erythro-l azido-2-hydroxy-l,2,3' propanetricarboxylic acid, trimethyl ester A solution of sodium azide (2.5 g.) in water (10 ml.) was added to a solution of (i)-erythro-l-mesyloxy-Z- hydroxy-l,2.3-propanetricarboxylic acid, trimethyl ester (6.56 g.) in ethanol (50 ml.). The reaction mixture was heated at reflux temperature for 2 hours then most of the solvent was removed in vacuo. The residue was dissolved in chloroform and the solution was washed with water (2 x), dried (MgSO and concentrated to dryness to give crude azide. The pure azide was obtained by crystallization from ether, mp 707 1.

Anal. Calcd. for C H N O C, 39.28; H, 4.76; N, 15.27.

Found: C, 39.48; H, 4.89; N, 15.20.

EXAMPLE 7 (:)-Erythro-l-amino-2-hydroxy-1,2,3- propanetricarboxylic acid. trimethyl ester, hydrochloride A solution ofthe crude (i)-erythro azide prepared as in Example 6 (4.9 g.) in methanol containing concentrated hydrochloric acid (1.33 ml.) was hydrogenated (50 p.s.i., RT) for 2 hours using 10% palladium on charcoal (800 mg.) as catalyst. The catalyst was removed by filtration of the reaction mixture through a bed of Celite. The filtrate was concentrated in vacuo and the resulting white solid was crystallized from methanol-ether to give the (i)-erythro-amine hydrochloride, mp 153-5. Recrystallization from methanolether furnished the analytically pure material, mp 1535.

Anal. Calcd. for C H NO HCI: C. 37.84.; H. 5.65; N, 4.90; 12.41. Found: C, 38.01; H, 5.90; N, 4.88;

EXAMPLE 8 (i)-Erythro-l-amino-2-hydroxy-1,2,3- propanetricarboxylic acid, lactam, dimethyl ester a. 2.6 g. Of the amine hydrochloride prepared as in Example 7 was placed in a 125 ml. Erlenmeyer flask under a slow stream of argon. The flask was immersed in a preheated oil bath (180) until the hydrochloride had melted and the effervesence had stopped (2-3 minutes). The oily residue was then dissolved in ethyl acetate (using a minimum amount of methanol to effect solution) and placed on a column of Florisil (60-100 mesh; 55 g.) and eluted with 2% methanol in ethyl acetate. The eluate (750 ml.) was concentrated in vacuo to give an oil which slowly solidified. Crystallization of the product from ethyl acetate-carbon tetrachloride yielded the lactam diester, mp 133135. Recrystallization from the same solvent afforded the analytical sample, mp 133.5135.5.

Anal. Calcd. for C,,H NO.,: C, 44.24; H, 11; Found: C, 44.54; H, .05;

b. To a stirred solution of the amine hydrochloride prepared as in Example 7 (571 mg.; 2.0 mmol) in dry methanol (10 ml.) was added a solution of potassium t-butoxide (225 mg.; 2.0 mmol) in dry methanol (10 ml.) to free the amine from its salt. The mixture containing the free amine was brought to reflux and maintained at that temperature for 3.5 hours. The cooled solution was decanted from the precipitated potassium chloride and the solvent was removed under reduced pressure. The residue was extracted with several portions (3 X 30 ml.) of hot ethyl acetate. The combined extracts were filtered to remove residual inorganic salts and then concentrated under reduced pressure. The oily residue solidified when triturated with ether to give lactam, mp 1247. This material was identical to the (i)-erythro lactam obtained above by pyrolysis of the amine hydrochloride.

EXAMPLE 9 (i)-Erythro-1-amino-2-hydroxy-1,2,3- propanetricarboxylic acid, 7 lactam Analv Calcd. for C H NO I C. 38.1 1: Found: C. 38.39;

EXAMPLE 10 l(S),2(S)-l-Amino-Z-hydroxy-l,2.3- propanetricarboxylic acid, trimethyl ester, hydrochloride [(+)-threo-amine hydrochloride] A solution of sodium azide (2.5 g.) in water 10 ml.) was added to a stirred solution of l(S).2(S)'1- mesyloxy-2-hydroxy-l,2,3-propane tricarboxylic acid, trimethyl ester [()-threo-mesylate] (6.56 g.) in ethanol (50 ml.). The reaction mixture was heated at reflux temperature for 45 minutes. then most of the solvent was removed in vacuo. The residue was diluted with water and extracted with chloroform (2 x The organic layers were washed with water, then were combined, dried (MgSO and concentrated under reduced pressure to give the crude ()-threo-azide as an oil; [01],, 54.0 (c, 1.0 MeOH).

A solution of the azide (5.8 g.) in methanol ml.) containing concentrated hydrochloric acid (1.8 ml.) was hydrogenated for 3 hours in a Parr Hydrogenator (48 psi; R.T.) using 10% palladium on charcoal (1.0 g.) as catalyst. The catalyst was removed by filtration of the reaction mixture through Celite and the filtrate was then evaporated in vacuo. The resulting solid residue was crystallized from methanol-ether to give 3.8 g. of the amine hydrochloride, mp 1646. Recrystallization from the same solvent mixture furnished the analytically pure specimen, mp l646; [a] 14.83 (c, 0.97, CH OH).

Anal. Calcd. for C,,H -,NO;.HCl: C, 37.84; H, 5.65; N, 4.90;

0112.41. Found: C; 37.71; H. 5.58; N, 4.76; Cl.l2.-13v

The following pharmaceutical formulations are illustrated for (:)-threo-l-amino- 2hydroxy-l.2,3-propanetricarboxylic acid, trimethyl ester, hydrochloride. These formulations are applicable PROCEDURE: 1. All of the ingredients were mixed until thoroughly blended in a suitable size container. 2. The powder was filled into No. 2, two piece. hard shell gelatin capsules to an approximate fill weight of 350 mg. using a Parke Davis capsulating machine. (Any similar type machine may be used.)

EXAM PLE l2 Tablet Formulation Per Tablet (i)-Threol 'amino-2-hydroxyl .l3-propanetricarboxylic acid. trimethyl ester. hydrochloride 200 mg. Dicalcium Phosphate Dihydrate. Unmilled 235 mg. Corn Starch 70 mg. FD 84 C Yellow No. 5 Aluminum Lake 25% 2 mg. Durkee 117 25 mg. Calcium Stearate 3 mg Total Weight 535 mg.

PROCEDURE:

1. All the ingredients were mixed thoroughly and Fitzed (Model D), using a No. 1A screen, medium speed. 2. The mixture was remixed and slugged.

3. The slugs were screened on an Oscillator through a No. 14 mesh screen and compressed on an E" machine.

EXAMPLE l3 Capsule Formulation Per Capsule (:)-Threo-l -amino-2-hydroxyl .2.3-propanetricarboxylic acid. trimethyl ester. hydrochloride Lactose. USP

Corn Starch. USP

Talc. USP

Total Weight LII No. lA screen with knives forward.

3. The blended powder was returned to the mixer, the tale added and blended thoroughly.

4. The mixture was filled into No. 4 hard shell gelatin capsules on a Parke Davis capsulating machine.

EXAMPLE 14 Tablet Formulation Per Tablet (i)-Threo-l -amino2hydroxy"1.2.3-pr0panetricarboxylic acid. trimethyl ester. hydrochloride 25 mg. Dicalcium Phosphate Dihydrate. Unmilled 175 mg. Corn Starch 24 mg. Magnesium Stearate l mg. Total Weight 225 mg.

PROCEDURE:

1. (i)-Threo-1-arnino-2-hydroxy-l,2,3-

propanetricarboxylic acid, trimethyl ester, hydrochloride and corn starch were mixed together and passed through a No. 00 screen in Model 1" Fitzmill with hammers forward.

2. This premix was then mixed with dicalcium phosphate and one-half of the magnesium stearate, passed through a No. 1A screen in Model J Fitzmill with knives forward. and slugged.

3. The slugs were passed through a No. 2A plate in a Model D Fitzmill at slow speed with knives forward, and the remaining magnesium stearate was added.

4. The mixture was mixed and compressed.

EXAMPLE l5 Tablet Formulation Per Tablet (i)Thre0- l -amino-2-hydroxyl ,2.3-propanetricarboxylic acid. triniethyl ester. hydrochloride 100 mg. Lactose. USP 202 mg. Corn Starch. USP mg. Amijel B01 1* 20 mg. Calcium Stearate 8 mg. Total Weight 4l0 mg.

"A prehydrolyzcd food grade corn starch. Any similar prcludroly zed corn starch may he used.

PROCEDURE:

1. (i)-Threo-l-amino-2-hydroxy-l.2,3- propanetricarboxylic acid, trimethyl ester, hydrochloride, lactose. corn starch. and Amijell 8011 were blended in a suitable mixer.

' 2. The mixture was granulated to a heavy paste with water and the moist mass was passed through a N0. 12 screen. It was then dried overnight at 1 10F.

3. The dried granules were passed through a No. 16 screen and transferred to a suitable mixer. The calcium stearate was added and mixed until uniform.

4. The mixture was compressed at a tablet weight of 410 mg. using tablet punches having a diameter of approximately 3/8 inch. (Tablets may be either flat or biconvex and may be scored if desired.)

EXAMPLE 16 Tablet Formulation Per Tablet (i)-Threol -amino-2-hydroxyl .2 .3-propanetricarboxylic acid. trimethyl ester. hydrochloride 500 mg. Corn Starch 30 mg. Lactose 88 mg. Gelatin 12 mg. Talcum 15 mg. Magnesium Stearate 5 mg. Total Weight 650 mg.

PROCEDU RE:

1. (i)-Threo-1-amino2-hydroxy-l ,2,3-

propanetricarboxylic acid, trimethyl ester, hydrochlo EXAMPLE 17 Measurement of lipogenesis in vivo Female Charles River rats weighing from 120-150 g. were provided free access to water and were fed a commercial diet prior to the initiation of the experiment. Each experimental group of animals were pre-fasted 2 days and then meal-fed a single meal daily from 9-12 a.m. for 7 to 13 days. The meal consisted ofa 70% glucose fat-free diet (G-70) containing 70% glucose. 24% vitamin-free casein, 5% salt and 1% vitamins, to which 40 g. cellulose was added per kilogram.

On the last day of feeding, 60 minutes prior to feeding, the aminocitric acid derivative in ASV of the composition sodium chloride 0.9%, carboxy methyl cellulose 0.5%, benzyl alcohol 0.86% and tween 80 (polyoxyethylene sorbitan monoleate) 0.39% was adminis-- tered by stomach tube. Immediately after feeding, rats were lightly anaesthetized with Penthrane (methoxyflurane) and injected in the tail vein with 0.25 ml. of a solution with the following composition: 12.3 mg. alanine, SpC C-aIanine (specific activity 156 mC/mmole) as fatty acid precursor and 30.6 mg. a-ketoglutarate as an transaminase acceptor dissolved in saline pH 7.4-7.6. After 30 minutes. rats were sacrificed by decapitation and their livers were excised, rapidly weighed, minced in 15 ml. water and homogenized in a Potter-Elvehjem homogenizer with five strokes of a drill press-driven teflon pestle. Duplicate 3 ml. aliquots of whole liver homogenates were added to tubes containing 2.1 ml. 5N NaOH and saponified with 2.6 ml. 5N H SO and extracted twice with 5 ml. of petroleum ether (bp 4060C.). Supernatants were added directly to glass counting vials, evaporated to dryness and 10 ml. of toluenePPO-POPOP scintillation fluid was added. Samples were analyzed for absolute activity in a Packard Tri-carb scintillation counter. Resulting data was expressed an nanomoles C-alanine incorporated/gram of tissue/30 minutes.

l(S),2(S)-l-Amino-2-hydroxy-1,2,3-

propanetricarboxylic acid trimethyl ester hydrochloride, when administered at 2.63 mmole/kg in ASV, gave the following results:

Nanomoles C-alanine/g. liver/30 min. Percent and the stereoisomers, optical antipodes and pharmaceutically acceptable salts thereof.

2. The compound of claim 1 wherein R is hydrogen, i.e. l-amino-2-hydroxy-l,2,3-propanetricarboxylic acid y lactam.

3. The threo isomer of the compound of claim 2.

4. The erythro isomer of the compound of claim 2.

5. The compound of claim 1 wherein R is lower alkyl.

6. The compound of claim 5 wherein R is methyl, i.e. l-amino-2-hydroxy-l,2,3-propanetricarboxylic acid 7 lactam, dimethyl ester.

7. The threo isomer of the compound of claim 6.

8. The erythro isomer of the compound of claim 6. 

1. A COMPOUND OF THE FORMULA
 2. The compound of claim 1 wherein R is hydrogen, i.e. 1-amino-2-hydroxy-1,2,3-propanetricarboxylic acid gamma lactam.
 3. The threo isomer of the compound of claim
 2. 4. The erythro isomer of the compound of claim
 2. 5. The compound of claim 1 wherein R is lower alkyl.
 6. The compound of claim 5 wherein R is methyl, i.e. 1-amino-2-hydroxy-1,2,3-propanetricarboxylic acid gamma lactam, dimethyl ester.
 7. The threo isomer of the compound of claim
 6. 8. The erythro isomer of the compound of claim
 6. 